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抗坏血酸是一种多功能微量营养素,灵长类动物缺乏其合成能力。

Ascorbate is a multifunctional micronutrient whose synthesis is lacking in primates.

作者信息

Fujii Junichi

机构信息

Department of Biochemistry and Molecular Biology, Graduate School of Medical Science, Yamagata University, Yamagata 990-9585, Japan.

出版信息

J Clin Biochem Nutr. 2021 Jul;69(1):1-15. doi: 10.3164/jcbn.20-181. Epub 2021 Mar 25.

Abstract

Ascorbate (vitamin C) is an essential micronutrient in primates, and exhibits multiple physiological functions. In addition to antioxidative action, ascorbate provides reducing power to α-ketoglutarate-dependent non-heme iron dioxygenases, such as prolyl hydroxylases. Demethylation of histones and DNA with the aid of ascorbate results in the reactivation of epigenetically silenced genes. Ascorbate and its oxidized form, dehydroascorbate, have attracted interest in terms of their roles in cancer therapy. The last step in the biosynthesis of ascorbate is catalyzed by l-gulono-γ-lactone oxidase whose gene is commonly mutated in all animals that do not synthesize ascorbate. One common explanation for this deficiency is based on the increased availability of ascorbate from foods. In fact, pathways for ascorbate synthesis and the detoxification of xenobiotics by glucuronate conjugation share the metabolic processes up to UDP-glucuronate, which prompts another hypothesis, namely, that ascorbate-incompetent animals might have developed stronger detoxification systems in return for their lack of ability to produce ascorbate, which would allow them to cope with their situation. Here, we overview recent advances in ascorbate research and propose that an enhanced glucuronate conjugation reaction may have applied positive selection pressure on ascorbate-incompetent animals, thus allowing them to dominate the animal kingdom.

摘要

抗坏血酸(维生素C)是灵长类动物必需的微量营养素,具有多种生理功能。除了抗氧化作用外,抗坏血酸还为脯氨酰羟化酶等α-酮戊二酸依赖性非血红素铁双加氧酶提供还原能力。在抗坏血酸的帮助下,组蛋白和DNA的去甲基化导致表观遗传沉默基因的重新激活。抗坏血酸及其氧化形式脱氢抗坏血酸在癌症治疗中的作用引起了人们的关注。抗坏血酸生物合成的最后一步由L-古洛糖酸-γ-内酯氧化酶催化,其基因在所有不合成抗坏血酸的动物中通常发生突变。对此种缺陷的一种常见解释是基于食物中抗坏血酸的可用性增加。事实上,抗坏血酸合成途径和通过葡萄糖醛酸结合进行的外源性物质解毒在代谢过程中共享直至尿苷二磷酸葡萄糖醛酸的过程,这引发了另一种假设,即不能合成抗坏血酸的动物可能已经发展出更强的解毒系统,以弥补它们缺乏产生抗坏血酸的能力,这将使它们能够应对自身状况。在这里,我们概述了抗坏血酸研究的最新进展,并提出增强的葡萄糖醛酸结合反应可能对不能合成抗坏血酸的动物施加了正选择压力,从而使它们在动物界占据主导地位。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6880/8325764/90b2f2cd443e/jcbn20-181f01.jpg

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